RS878854417 HECW2

Health Risk Chr 2:196225800
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neurodevelopmental disorder with hypotonia
seizures
and absent language
Inborn genetic diseases
Neurodevelopmental disorder with progressive microcephaly
spasticity
and brain anomalies
HECW2-related disorder
Neurodevelopmental disorder with hypotonia
seizures
and absent language
Inborn genetic diseases
Neurodevelopmental disorder with progressive microcephaly
spasticity
and brain anomalies
Other Variants in HECW2
rs878854416 rs878854422 rs143511416 rs1057524302 rs770779546 rs1553629086 rs774316240 rs1553633403 rs1553635778 rs1553496847
Ask Dr. Hemsworth about this variant